Department of Orthopaedic Surgery, McKay Orthopaedic Research Laboratory, University of Pennsylvania, Philadelphia, PA, USA; School of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA, USA; Translational Musculoskeletal Research Center, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, USA.
Department of Orthopaedic Surgery, McKay Orthopaedic Research Laboratory, University of Pennsylvania, Philadelphia, PA, USA; Translational Musculoskeletal Research Center, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, USA.
Osteoarthritis Cartilage. 2019 Dec;27(12):1860-1869. doi: 10.1016/j.joca.2019.07.016. Epub 2019 Aug 13.
The objective of this study was to perform a quantitative analysis of the structural and functional alterations in the intervertebral disc during in vivo degeneration, using emerging tools that enable rigorous assessment from the microscale to the macroscale, as well as to correlate these outcomes with noninvasive, clinically relevant imaging parameters.
Degeneration was induced in a rabbit model by puncturing the annulus fibrosus (AF) with a 16-gauge needle. 2, 4, 8, and 12 weeks following puncture, degenerative changes in the discs were evaluated via magnetic resonance imaging (MRI), whole motion segment biomechanics, atomic force microscopy, histology and polarized light microscopy, immunohistochemistry, biochemical content, and second harmonic generation imaging.
Following puncture, degeneration was evident through marked changes in whole disc structure and mechanics. Puncture acutely compromised disc macro and microscale mechanics, followed by progressive stiffening and remodeling. Histological analysis showed substantial anterior fibrotic remodeling and osteophyte formation, as well as an overall reduction in disc height, and disorganization and infolding of the AF lamellae into the NP space. Increases in NP collagen content and aggrecan breakdown products were also noted within 4 weeks. On MRI, NP T2 was reduced at all post-puncture time points and correlated significantly with microscale indentation modulus.
This study defined the time dependent changes in disc structure-function relationships during IVD degeneration in a rabbit annular injury model and correlated degeneration severity with clinical imaging parameters. Our findings identified AF infolding and occupancy of the space as a principle mechanism of disc degeneration in response to needle puncture, and provide new insights to direct the development of novel therapeutics.
本研究旨在通过新兴工具对活体退变过程中椎间盘的结构和功能改变进行定量分析,这些工具能够从微观尺度到宏观尺度进行严格评估,并将这些结果与非侵入性、临床相关的影像学参数相关联。
通过 16 号针穿刺纤维环(AF)在兔模型中诱导退变。在穿刺后 2、4、8 和 12 周,通过磁共振成像(MRI)、全运动节段生物力学、原子力显微镜、组织学和偏光显微镜、免疫组织化学、生化含量和二次谐波产生成像来评估椎间盘的退行性变化。
穿刺后,整个椎间盘结构和力学的明显变化表明发生了退变。穿刺急性损害了椎间盘的宏观和微观力学,随后出现逐渐僵硬和重塑。组织学分析显示前纤维性重塑和骨赘形成明显,椎间盘高度总体降低,AF 板层组织紊乱并折叠到 NP 空间。还在 4 周内观察到 NP 胶原含量和聚集蛋白聚糖分解产物增加。在 MRI 上,NP T2 在所有穿刺后时间点均降低,与微尺度压痕模量显著相关。
本研究在兔环状损伤模型中定义了椎间盘结构-功能关系在 IVD 退变过程中的时间依赖性变化,并将退变严重程度与临床影像学参数相关联。我们的发现确定了 AF 内折和 NP 空间占据是针对针穿刺的椎间盘退变的主要机制,并为指导新型治疗药物的开发提供了新的见解。